-
Selected samples from the Boston Children's Hospital Childrens Rare Disease Cohorts initiative
Dataset
EGAD00001006179
-
RNA-seq of Bone Metastasis from breast and prostate cancers
Dataset
EGAD00001006356
-
Small RNA sequencing from CSF extracellular vesicles - PD/CTR
Dataset
EGAD00001006629
-
BLUEPRINT September 2016, ATAC-seq for venous blood, on Genome GRCh38
Dataset
EGAD00001002709
-
SEQCAP_Internation_1q_Type_2_Consortium - Agilent SureSelec
Dataset
EGAD00001000421
-
BLUEPRINT release August 2016, DNase-Hypersensitivity for macrophage - T=6days B-glucan, on genome GRCh38
Dataset
EGAD00001002425
-
Abnormal foetal development exome trios
Dataset
EGAD00001001442
-
Tumor mutational burden (TMB) calculated on bladder tumor pre-treatment DNA sequencing data
Dataset
EGAD00001006851
-
RNA-seq TPM matrices
Dataset
EGAD00001006741
-
BLUEPRINT: RNA-seq of progenitor cells
Dataset
EGAD00001000745
-
Single cell mRNA sequencing of CD11b cells from a primary GBM - SF 10360i
Dataset
EGAD00001003111
-
Whole exome Sequencing (WES) of multiple tumor biopsies, patient-derived spheroids and leukocyte DNA from colorectal cancer patients (BAM files)
Dataset
EGAD00001003821
-
Single-cell RNA-seq of immune cells from Melanoma tumors (Li et al, 2018)
Dataset
EGAD00001004497
-
RNA sequencing of tumor samples from patients with Waldenstrom macroglobulinemia
Dataset
EGAD00001005324
-
Pleomorphic invasive lobular carcinoma targeted exome sequencing
Dataset
EGAD00001003995
-
Exome sequencing of a novel cervical cancer cell line
Dataset
EGAD00001004480
-
RNA-seq data of 370 high grade ovarian tumors from the ICON7 trial
Dataset
EGAD00001004988
-
Whole-exome and whole-genome sequencing data
Dataset
EGAD00001005087
-
Gene panel sequencing of paired samples from primary and relapsed IDH-wt glioblastomas
Dataset
EGAD00001004565
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW46_F
Dataset
EGAD00001001824
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW14_C
Dataset
EGAD00001001787
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB62_M
Dataset
EGAD00001001780
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB58_C
Dataset
EGAD00001001772
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB52_C
Dataset
EGAD00001001763
-
WXS files for paper titled 'Genomic Landscape of Pediatric Myelodysplastic Syndromes'
Dataset
EGAD00001003781
-
Common clonal origin of chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia in a patient with a germline CHEK2 variant
Dataset
EGAD00001007644
-
BLUEPRINT release August 2016, RNA-Seq for monocyte - T=0days, on genome GRCh38
Dataset
EGAD00001002360
-
Whole Exome Sequencing
Dataset
EGAD00001004352
-
BLUEPRINT release August 2015, DNase-Hypersensitivity for inflammatory macrophage, on genome GRCh38
Dataset
EGAD00001001573
-
Exome sequencing of serially transplanted genetically marked IC-enriched primary PDAC cultures.
Dataset
EGAD00001000884
-
Exome sequencing of tumor DNA samples from patients with BPLL
Dataset
EGAD00001004410
-
BLUEPRINT release August 2015, RNA-Seq for plasma cell, on genome GRCh38
Dataset
EGAD00001001523
-
BLUEPRINT release August 2015, RNA-Seq for monocyte - None, on genome GRCh38
Dataset
EGAD00001001532
-
SPECTA: NGS Screening Program for Efficient Clinical Trial Access
Dataset
EGAD00001000894